via Hgershoff reaction or Cu catalyzed intramolecular C-S bond - PowerPoint PPT Presentation

Synthesis of bioactive 2-(arylamino)thiazolo[5,4-f] quinazolin-9-ones via Hügershoff reaction or Cu catalyzed intramolecular C-S bond formation Damien Hédou 1 , Carole Dubouilh 1 , Nadège Loaëc 2,3 , Laurent Meijer 3 , Corinne Fruit 1 and Thierry Besson 1,* 1 Normandie Univ, UNIROUEN, INSA Rouen, CNRS, COBRA, 76000 Rouen, France; 2 Protein Phosphorylation & Human Disease group, Station Biologique, 29680 Roscoff, France 3 Manros Therapeutics, Centre de Perharidy, 29680 Roscoff, France 1 * Corresponding author: thierry.besson@univ-Rouen.fr

Synthesis of bioactive 2-(arylamino)thiazolo[5,4-f] quinazolin-9-ones via Hügershoff reaction or Cu catalyzed intramolecular C-S bond formation. 2

Abstract: A library of thirty eight novel thiazolo[5,4- f ]quinazolin-9(8 H )-one derivatives (series 8 , 10 , 14 and 17 ) was prepared via the Hügershoff reaction and a Cu catalyzed intramolecular C-S bond formation, helped by microwave-assisted technology when required. The efficient multistep synthesis of the key 6-amino-3- cyclopropylquinazolin-4(3 H )-one ( 3 ) has been reinvestigated and performed on a multi-gram scale from the starting 5-nitroanthranilic acid. The inhibitory potency of the final products was evaluated against five kinases involved in Alzheimer’s disease and showed that some molecules of the 17 series described in this paper are particularly promising for the development of novel multi-target inhibitors of kinases. Keywords: Hügershoff reaction; thiazolo[5,4-f ]quinazolin-9(8H)-ones; microwave- assisted synthesis; protein kinases 3

Introduction Our research group is mainly invested in the synthesis of C,N,S-containing bioactive molecules able to modulate the activity of deregulated kinases (CDK5, GSK-3, CLK1, CK1 and the dual-specificity kinase DYRK1A) involved to some extent in Alzheimer’s disease (AD). Among them some thiazolo[5,4- f ]quinazolin-9(8 H )- ones (Figure 1) have been revealed of particular interest in the design of multi- target-directed ligands (MTDLs), a new strategy for the development of new tools against neurodegenerative diseases. The target molecules were thiazolo[5,4- f ]quinazolin-9-ones substituted in position N-8 by a cyclopropyl chain (Figure 1). Figure 1. General formula of lead kinases inhibitors previously described [1-5] and new molecules targeted. 4

Results and discussion : Envisioned r etrosynthetic pathway and the key 6-amino-3- cyclopropylquinazolin-4(3H)-one ( 3 ). The first planned strategy uses the Hügershoff reaction, a bromine-mediated cyclization process involving electrophilic addition. The second route imagined concerns a metal catalyzed intramolecular C-S bond formation on the synthesis of variously 2-substituted benzothiazoles from thiobenzanilides (Scheme 1). Scheme 1. Envisioned retrosynthetic pathway for the synthesis of the target products, via Hügershoff reaction or transition metal-catalyzed intramolecular C-S bond formation. 5

Results and discussion: Synthesis of the key 6-amino-3-cyclopropylquinazolin-4(3H)- one ( 3 ). The key 6-amino-3-cyclopropylquinazolin-4(3 H )-one ( 3 ) was obtained via an efficient microwave-assisted MCR procedure. Scheme 2. Sequential MCR procedure for convenient synthesis of 6-amino-3-cyclopropylquinazolin-4(3 H )-one ( 3 ) from 1 . Reagents and conditions: ( a ) Step 1: DMFDMA (2.5 equiv), DMF, 100 ° C (µw), 15 min; Step 2: Cyclopropylamine (1.1 eq), AcOH, 100 ° C (µw), 15 min; 85%; ( b ) HCO 2 NH 4 (5.0 equiv), Pd/C (10%), EtOH, 85 ° C ( μw ), 15 min; 85%. 6

Results and discussion : Synthesis of 2-aminoarylthiazolo[5,4-f]quinazolin-9-ones via Hügershoff reaction Synthetic routes for access to the key isothiocyanate 4. Route 1 : with thiophosgene Appel salt Route 2 : via Appel salt chemistry 7

Results and discussion : Synthesis of thiourea 7a-l from amine 3 or from isothiocyanate 4 . 8

Results and discussion : Synthesis of 2-aminoarylthiazolo[5,4-f]quinazolin-9-ones via Hügershoff reaction. The cyclization was not regioselective. The phenyl group (A) of the starting diaryl thiourea 7a possessed the most electron-rich ortho -carbon, compared to the quinazolin-4-one ring B. Compounds 10 are the major products. 9

Results and discussion : Synthesis of 2-aminoarylthiazolo[5,4-f]quinazolin-9-ones via Hügershoff reaction. a Isolated yield. b Traces of compounds of the 9 series were detected but not purified Electron-deficient phenyl substituents are present in A cycle of the thiourea derivatives. 10

Results and discussion : Synthesis of 2-aminoaryl- and 2-aminoalkylthiazolo[5,4- f]quinazolin-9-ones via Metal Catalyzed C-S Bond Formation. Synthesis of thiourea 12 via condensation of aniline with isothiocyanate 13 . Formation of the isothiocyanate function was performed before bromination of the skeleton 11

Results and discussion : Synthesis of 2-aminoaryl- and 2-aminoalkylthiazolo[5,4- f]quinazolin-9-ones via Metal Catalyzed C-S Bond Formation A sequential one-pot version of the transformation of isothiocyanate 13 into the tricyclic arene 8 series was considered. This approach required the complete conversion of the starting material 13 into the corresponding thiourea intermediate (in square brackets) before addition of other reagents (CuI and Cs 2 CO 3 ) and microwave-assisted cyclization by heating for 1 h. 12

Results and discussion : Synthesis of 2-aminoaryl- and 2-aminoalkylthiazolo[5,4- f]quinazolin-9-ones via Metal Catalyzed C-S Bond Formation. Depending on the nature of aniline, the conversion time can vary from 30 min (electron-rich compounds e.g. 4-OMe, 3,4-diOMe or 4-NMe 2 anilines) to an overnight stirring (12 h). Because electron-poor anilines required several hours for completion of the first part of the reaction, the Hügershoff reaction was found to be more efficient in these cases (products 8d – f ). 13

Results and discussion : Synthesis of 2-aminoaryl- and 2-aminoalkylthiazolo[5,4- f]quinazolin-9-ones via Metal Catalyzed C-S Bond Formation. Microwave-assisted heating at 80 ° C for 1 h complete the sequence to afford the expected cyclized compounds (series 14a – f ) in very good yields (80% – 96%, see Table 5). 14

Results and discussion : Synthesis of carboximidamides 17a-f from brominated amine 11 . - Regio-selective intramolecular C-S coupling-reaction, catalyzed by CuI. - A one-pot sequential process helped by microwave-assisted heating. It allowed the convenient synthesis of new thiazoloquinazolin-9- ones. 15

Results and discussion : Kinase inhibitory activity a,b,c of the thiazolo[5,4- f ]quinazoline series ( 7a-l , 8a-m , 10a and 10l , 14a-f and 17a-f ). All compounds were first tested at a Compounds CDK5/p25 CK1d/e CLK1 DYRK1A GSK-3a/b final concentration of 10 µM. 7a-l >10 >10 >10 >10 ≥10 Compounds showing less than 50% 8a >10 >10 3.4 >10 ≥10 inhibition were considered as inactive 8c-f >10 >10 >10 >10 ≥10 (IC 50 >10 µM). Compounds displaying 8g >10 >10 1.7 >10 ≥10 more than 50% inhibition at 10 µM 8h-i >10 >10 >10 >10 ≥10 8j >10 >10 1.3 2.0 7.3 were next tested over a wide range of 8k-m >10 >10 >10 >10 ≥10 concentrations (usually 0.01 to 10 µM), 10a >10 >10 5.2 4.8 ≥10 and IC 50 values were determined from 10l >10 >10 >10 >10 ≥10 the dose-response curves (Sigma-Plot). 14a >10 >10 3.4 >10 >10 b -carboline Harmine is a alkaloid 14b >10 >10 >10 >10 ≥10 known to be a potent inhibitor of 14c >10 >10 >10 >10 ≥10 14d >10 >10 8.1 8.2 ≥10 DYRK1A. It was also tested as positive 14e >10 >10 5.3 >10 ≥10 control and its IC 50 values were >10 >10 >10 >10 ≥10 14f compared to those obtained for the 17a >10 >10 1.0 0.67 0.4 compounds under study. >10 >10 0.29 4.4 1.1 17b 17c >10 >10 2.3 3.2 2.8 >10 >10 2.1 2.9 3.9 17d 17e >10 1.9 0.38 0.14 0.23 The two most active molecules 17f >10 >10 0.61 0.82 0.49 Harmine >10 1.5 0.026 0.029 >10 a IC 50 values are reported in μM . The most significant results are presented in bold; b Kinases activities were assayed in triplicate. Typically, the standard deviation of single data points was below 10%. 16

Results and discussion : The two most active molecules : 17e and 17f Comparing the results of 2-aminosubstituted derivatives and their carboximidamides analogs, it seems rather obvious that having such molecular scafolds with submicromolar affinities for various kinases is related to the presence of carboximidamide or carboximidate functions that result from the substitution of a carbonitrile group itself present in position 2 of the thiazole. 17

Conclusion - A library of 38 novel 8-aminoaryl thiazolo[5,4- f ]quinazolin-9(8 H )-ones ( 8 , 10 , 14 and 17 series) has been prepared, using microwave-assisted technology: - An efficient multistep synthesis of the key 6-amino-3-cyclopropylquinazolin-4(3 H )- one ( 3 ) was developed and optimized to the multigram scale. - The Hügershoff reaction was re-investigated under microwaves. - A CuI catalyzed ligand-free intramolecular C-S bond formation was also developed. - Molecules of the 8 , 10 and 14 series described in this paper are not pertinent for the development of kinases inhibitors. - The most active compounds are carboximidamides analogues ( 17 series) of the target compounds that shown submicromolar IC 50 values for CLK1, DYRK1A and GSK-3 a / b over the other tested enzymes. 18